Canonical Allele Identifier: CA2263919402
Gene: COL1A1 HGNC NCBI

Linked Data

dbSNP Id: rs1907627080

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50196727A>G , CM000679.2:g.50196727A>G GRCh38
NC_000017.10:g.48274088A>G , CM000679.1:g.48274088A>G GRCh37
NC_000017.9:g.45629087A>G NCBI36
NG_007400.1:g.9913T>C , LRG_1:g.9913T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.805-57T>C MANE Select ENSP00000225964.6:n.805-57T>C
ENST00000225964.9:c.805-57T>C ENSP00000225964.5:n.805-57T>C
ENST00000495677.1:n.532-57T>C
NM_000088.3:c.805-57T>C , LRG_1t1:c.805-57T>C NP_000079.2:n.805-57T>C
XM_005257058.3:c.805-57T>C XP_005257115.2:n.805-57T>C
XM_005257059.3:c.805-57T>C XP_005257116.2:n.805-57T>C
XM_011524341.1:c.805-57T>C XP_011522643.1:n.805-57T>C
XM_005257058.4:c.805-57T>C XP_005257115.2:n.805-57T>C
XM_005257059.4:c.805-57T>C XP_005257116.2:n.805-57T>C
NM_000088.4:c.805-57T>C MANE Select NP_000079.2:n.805-57T>C